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510(k) Data Aggregation

    K Number
    K971044
    Date Cleared
    1997-08-25

    (157 days)

    Product Code
    Regulation Number
    880.6250
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    A patient exam glove is a disposable device intended to be worn on the examiner's hand to prevent contamination between patient and examiner.

    Device Description

    Not Found

    AI/ML Overview

    The provided documents are a 510(k) clearance letter from the FDA for medical gloves. This type of document does not contain any information about acceptance criteria, device performance studies, sample sizes, ground truth establishment, or expert qualifications in the context of an AI/ML medical device.

    The letter explicitly states that the device is "substantially equivalent" to predicate devices, meaning it has similar indications for use, technological characteristics, and safety and effectiveness. The entire review focuses on regulatory compliance and substantial equivalence, not on the detailed performance characteristics or studies typically associated with AI/ML device evaluations.

    Therefore, I cannot provide the requested information based on the input document.

    To answer your request, I would need a document describing the testing and validation of an AI/ML medical device, which would typically include details such as clinical study protocols, performance metrics, and statistical analysis.

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    K Number
    K955425
    Date Cleared
    1996-12-30

    (398 days)

    Product Code
    Regulation Number
    880.6250
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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